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rs10493256

From SNPedia

Orientationminus
Stabilizedminus
Make rs10493256(A;A)
Make rs10493256(A;G)
Make rs10493256(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position59223276
is asnp
is mentioned by
dbSNPrs10493256
ebirs10493256
HLIrs10493256
Exacrs10493256
Varsomers10493256
Maprs10493256
PheGenIrs10493256
hapmaprs10493256
1000 genomesrs10493256
hgdprs10493256
ensemblrs10493256
gopubmedrs10493256
geneviewrs10493256
scholarrs10493256
googlers10493256
pharmgkbrs10493256
gwascentralrs10493256
openSNPrs10493256
23andMers10493256
23andMe allrs10493256
SNP Nexus

SNPshotrs10493256
SNPdbers10493256
MSV3drs10493256
GWAS Ctlgrs10493256
GMAF0.1708
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs10493256 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have been found to be overrepresented in 1,152 patients with sporadic amyotrophic lateral sclerosis (ALS).[PMID 17671248]

[PMID 19125359] appears to increase the risk of developing sporadic ALS in our Chinese population

[PMID 19177248] A study involving a large case-control series from the Netherlands, Belgium, Sweden and Ireland (total: 1883 sporadic ALS patients and 2063 controls) found no significant association between sporadic ALS and the six previously reported associated SNPs, including this one.


[PMID 19922123] Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China


[PMID 19922138] Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis